18 results match your criteria: "Fondazione IRCCS Policlinico S. Matteo and University of Pavia[Affiliation]"
J Cardiovasc Med (Hagerstown)
July 2022
Department of Molecular and Translational Medicine, University of Brescia, Italy.
Background: Several risk factors have been identified to predict worse outcomes in patients affected by SARS-CoV-2 infection. Machine learning algorithms represent a novel approach to identifying a prediction model with a good discriminatory capacity to be easily used in clinical practice. The aim of this study was to obtain a risk score for in-hospital mortality in patients with coronavirus disease infection (COVID-19) based on a limited number of features collected at hospital admission.
View Article and Find Full Text PDFNutrients
October 2021
Pediatric Department, "Vittore Buzzi" Children's Hospital, 20154 Milan, Italy.
Childhood obesity rates have dramatically risen in numerous countries worldwide. Obesity is likely a factor in increased asthma risk, which is already one of the most widespread chronic respiratory pathologies. The pathogenic mechanism of asthma risk has still not yet been fully elucidated.
View Article and Find Full Text PDFChildren (Basel)
June 2021
Pediatric Department, "Vittore Buzzi" Children's Hospital, 20154 Milano, Italy.
In the last few decades, obesity has increased dramatically in pediatric patients. Obesity is a chronic disease correlated with systemic inflammation, characterized by the presence of CD4 and CD8 T cell infiltration and modified immune response, which contributes to the development of obesity related diseases and metabolic disorders, including impaired glucose metabolism. In particular, Treg and Th17 cells are dynamically balanced under healthy conditions, but imbalance occurs in inflammatory and pathological states, such as obesity.
View Article and Find Full Text PDFCase Rep Pediatr
March 2021
Department of Pediatrics, Children's Hospital "V. Buzzi", 20157 Milano, Italy.
Background: Classical salt-wasting (SW) congenital adrenal hyperplasia (CAH) and Gitelman syndrome (GS) are two genetic conditions in which dyselectrolytemia may occur. No association between the two conditions has been previously described. .
View Article and Find Full Text PDFEur J Heart Fail
December 2020
Cardiology, ASST Spedali Civili di Brescia and Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy.
Aims: To assess the prognostic value of a history of heart failure (HF) in patients with coronavirus disease 2019 (COVID-19).
Methods And Results: We enrolled 692 consecutive patients admitted for COVID-19 in 13 Italian cardiology centres between 1 March and 9 April 2020. Mean age was 67.
Clin Res Cardiol
July 2021
Cardiology, ASST Spedali Civili and Department of Medical and Surgical Specialties, Radiological Sciences and Public Health, University of Brescia, Brescia, Italy.
J Pediatr Endocrinol Metab
May 2020
Pediatric and Adolescent Unit, Department of Internal Medicine, University of Pavia, Pavia, Italy.
Objectives Data on the predictive values of parameters included in the diagnostic work-up for precocious puberty (PP) remain limited. We detected the diagnostic value of basal sex hormone levels, pelvic ultrasound parameters and bone age assessment for activation of the hypothalamic-pituitary-gonadal axis in girls with PP, in order to help in the decision to perform GnRH testing. Patients and methods We retrospectively considered 177 girls with PP.
View Article and Find Full Text PDFRadiother Oncol
June 2020
Radiation Oncology Department, University and Spedali Civili of Brescia, Italy.
Clin Case Rep
August 2018
In patients with autoimmune disease, gynecomastia should not be considered as 1 of the first signs of hyperthyroidism, rather it is a breast pathology that can be present even when euthyroidism restoration is achieved. It is unknown whether the autoimmune nature of thyroid disorders or simply the hyperthyroidism effects breast changes.
View Article and Find Full Text PDFHematol Oncol
December 2018
Radiation Oncology Unit, Fondazione IRCCS Policlinico S. Matteo, Pavia, Italy.
Follicular lymphoma (FL) is the most common subtype of indolent non-Hodgkin lymphoproliferative disorders. Treatment strategies for FL may include several therapeutic choices, ranging from a "watchful waiting" approach to stem cell transplantation, mostly depending on staging, age, risk factors, and disease burden at diagnosis. The high radiosensitivity of FL compared with other solid tumors has been known since the beginning of radiotherapy treatment in lymphoma patients.
View Article and Find Full Text PDFAnn Transplant
September 2017
Department of Internal Medicine and Therapeutics, Unit of Cellular and Molecular Pharmacology and Toxicology, University of Pavia, Pavia, Italy.
BACKGROUND Ischemic cholangitis is the main cause of liver failure after transplantation and subnormothermic machine perfusion may represent a better strategy than conventional cold storage, minimizing preservation injury. We compared livers preserved by machine perfusion at 20°C (MP20) or by cold storage at 4°C (CS4) with regard to hypoxia-inducible factor (HIF)-1α mRNA expression and protein stabilization in hypoxic conditions. MATERIAL AND METHODS Livers from male Wistar rats were stored on ice at 4°C in UW solution (CS4) or perfused with oxygenated Krebs-Henseleit buffer at 20°C (MP20) for six hours.
View Article and Find Full Text PDFPediatr Blood Cancer
August 2017
Human and Medical Genetics, Department of Clinical and Experimental Medicine, University of Insubria, Varese, Italy.
Background: Two chromosome anomalies are frequent in the bone marrow (BM) of patients with Shwachman-Diamond syndrome (SDS): an isochromosome of the long arm of chromosome 7, i(7)(q10), and an interstitial deletion of the long arm of chromosome 20, del(20)(q). These anomalies are associated with a lower risk of developing myelodysplasia (MDS) and/or acute myeloid leukemia. The chromosome anomalies may be due to an SDS-specific karyotype instability, reflected also by anomalies that are not clonal, but found in single cells in the BM or in peripheral blood (PB).
View Article and Find Full Text PDFMol Cell Biochem
August 2016
Department of Internal Medicine and Therapeutics, University of Pavia, Via Ferrata 9A, 27100, Pavia, Italy.
Using an experimental model of NASH induced by a methionine-choline-deficient (MCD) diet, we investigated whether changes occur in serum and tissue levels of asymmetric dimethylarginine (ADMA). Male Wistar rats underwent NASH induced by 8-week feeding with an MCD diet. Serum and hepatic biopsies at 2, 4 and 8 weeks were taken, and serum enzymes, ADMA and nitrate/nitrite (NOx), were evaluated.
View Article and Find Full Text PDFFetal Pediatr Pathol
October 2016
e Pediatric Unit, University of Pavia and Fondazione IRCCS Policlinico San Matteo, Pavia , Italy.
Objective: Prenatal heart adaptations to congenital diaphragmatic hernia (CDH) could help define postnatal outcome.
Methods: We retrospectively analyzed post-mortem tissues from fetuses with severe CDH (n = 7). Histology and immunohistochemical distribution of desmin, muscle actin [HHF35], endothelin-1 [ET-1] and TGF-β were evaluated.
J Transl Med
November 2015
Vascular Surgery Unit, Fondazione IRCCS Policlinico S. Matteo and University of Pavia, Piazzale Golgi 19, 27100, Pavia, Italy.
Objectives: Demonstrate the safety and effectiveness of highly purified CD133+ autologous stem cells in critical limb ischemia (CLI).
Design: Prospective single-center not randomized. Clinicaltrials.
Int Rev Immunol
February 2015
Unit of Nephrology, Dialysis and Transplantation, Fondazione IRCCS Policlinico S. Matteo and University of Pavia, Pavia , Italy.
Costimulatory pathways play a key role in immunity, providing the second signal required for a full activation of adaptive immune response. Different costimulatory families (CD28, TNF-related, adhesion and TIM molecules), characterized by structural and functional analogies, have been described. Costimulatory molecules modulate T cell activation, B cell function, Ig production, cytokine release and many other processes, including atherosclerosis.
View Article and Find Full Text PDFEur J Haematol
October 2013
Unit of Nephrology, Dialysis and Transplantation, Fondazione IRCCS Policlinico S.Matteo and University of Pavia, Pavia, Italy.
Haemophilia A and B are genetic X-linked bleeding disorders, caused by mutations in genes encoding factors VIII and IX, respectively. Clinical manifestations of haemophilia are spontaneous haemorrhage or acute bleeding caused by minor trauma, resulting in severe functional consequences that can culminate in a debilitating arthropathy. Life expectancy and quality of life of patients with haemophilia have dramatically improved over the last years, mainly for new therapeutic options and the awareness to the risk of HCV and HIV infections.
View Article and Find Full Text PDFEur J Heart Fail
August 2007
Division of Cardiology, Fondazione IRCCS Policlinico S. Matteo and University of Pavia, 27100 Pavia, Italy.
Background: Patients with AL amyloidosis often present with signs of congestive heart failure.
Aim: This study was prospectively designed to assess the significance of RV dysfunction in AL amyloidosis.
Methods And Results: Seventy-four patients with biopsy proven AL amyloidosis underwent a thorough echocardiographic evaluation.